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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906538Generated: October 25, 2026

Tetrahydrofuran → 3-Diphenylmethoxycarbonyl-1-(2-benzyloxycarbonylamino-4-thiazolyl)-2-propene-1,1-dicarboxylic acid diethyl ester

https://huagongshe.com/reaction/1906538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactanttrans-3-Chloroacrylic acidHCID 638124—
Reactant2-(2-Benzyloxycarbonylamino-4-thiazolyl)malonic acid diethyl esterHCID 13671424—
SolventHydrochloric AcidHCID 313—
SolventEthyl AcetateHCID 8857—
Product3-Diphenylmethoxycarbonyl-1-(2-benzyloxycarbonylamino-4-thiazolyl)-2-propene-1,1-dicarboxylic acid diethyl esterHCID 54124382—

Reaction Steps

To a solution of 2-(2-benzyloxycarbonylamino-4-thiazolyl)malonic acid diethyl ester in tetrahydrofuran (20 parts) are added sodium hydride (2.35 equivalents) and a solution of trans-3-chloroacrylic acid diphemylmethyl ester (1.2 equivalents) in tetrahydrofuran (8 parts) under ice cooling. After stirring at 35° to 40° C. for 12.5 hours, the mixture is diluted with ethyl acetate and diluted hydrochloric acid, washed with water, dried, and concentrated. The residue is chromatographed over silica gel. The fraction eluted with a mixture of benzene and ethyl acetate (15:1) is crystallized from ethyl acetate to give 3-diphenylmethoxycarbonyl-1-(2-benzyloxycarbonylamino-4-thiazolyl)-2-propene-1,1-dicarboxylic acid diethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04652652
Source datasetuspto-grants-1987_03
ORD IDord-b2a4fb4ac36a474cb71c797adfe8b550
Source noteuspto-grants-1987_03